A Long-term Safety Study of Once-daily Travatan

Overview

Long term safety study of TRAVATAN in patients with Open-angle glaucoma or ocular hypertension.

Full Title of Study: “A Long-term Safety Study of Once-daily TRAVATAN”

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: Non-Randomized
    • Intervention Model: Single Group Assignment
    • Primary Purpose: Treatment
    • Masking: None (Open Label)
  • Study Primary Completion Date: March 2009

Interventions

  • Drug: Travatan
    • Travoprost (0.004%) 1 drop each eye once daily

Arms, Groups and Cohorts

  • Experimental: Travatan
    • Travoprost (0.004%)

Clinical Trial Outcome Measures

Primary Measures

  • Mean Intraocular Pressure
    • Time Frame: At 5 years.
    • Mean IOP for the patient’s worse eye at baseline was used in the secondary endpoint analysis. 2 consecutive IOP measurements for each eye were taken. If the 2 measurements for the same eye differ by 4 mmHg or less, the average of the measurements would be considered as the mean IOP for that eye. If the 2 measurements for the same eye differ by more than 4 mmHg, then a third measurement was to be taken. All IOP measurements were performed with a Goldmann applanation tonometer.

Participating in This Clinical Trial

Adult patients of any race and either sex with chronic angle-closure glaucoma.

Gender Eligibility: All

Minimum Age: 18 Years

Maximum Age: N/A

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • Alcon Research
  • Provider of Information About this Clinical Study
    • Sponsor

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